Canonical Allele Identifier: CA216884043

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.535463G>A , CM000673.2:g.535463G>A	GRCh38
NC_000011.9:g.535463G>A , CM000673.1:g.535463G>A	GRCh37
NC_000011.8:g.525463G>A	NCBI36
NG_007666.1:g.5088C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005343.4:c.-101C>T (HRAS) MANE Select	NP_005334.1:n.-101C>T
ENST00000311189.8:c.-101C>T (HRAS) MANE Select	ENSP00000309845.7:n.-101C>T
NM_176795.5:c.-101C>T (HRAS) MANE Plus Clinical	NP_789765.1:n.-101C>T
ENST00000417302.7:c.-101C>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.-101C>T
NM_001130442.1:c.-101C>T (HRAS)	NP_001123914.1:n.-101C>T
NM_001130442.2:c.-101C>T (HRAS)	NP_001123914.1:n.-101C>T
NM_001130442.3:c.-101C>T (HRAS)	NP_001123914.1:n.-101C>T
NM_001318054.1:c.-420C>T (HRAS)	NP_001304983.1:n.-420C>T
NM_001318054.2:c.-420C>T (HRAS)	NP_001304983.1:n.-420C>T
NM_005343.2:c.-101C>T (HRAS)	NP_005334.1:n.-101C>T
NM_005343.3:c.-101C>T (HRAS)	NP_005334.1:n.-101C>T
NM_176795.3:c.-101C>T (HRAS)	NP_789765.1:n.-101C>T
NM_176795.4:c.-101C>T (HRAS)	NP_789765.1:n.-101C>T
ENST00000311189.7:c.-101C>T (HRAS)	ENSP00000309845.7:n.-101C>T
ENST00000417302.5:c.-101C>T (HRAS)	ENSP00000388246.1:n.-101C>T
ENST00000417302.6:c.-101C>T (HRAS)	ENSP00000388246.1:n.-101C>T
ENST00000451590.5:c.-101C>T (HRAS)	ENSP00000407586.1:n.-101C>T
ENST00000462734.2:c.-54+873C>T (HRAS)	ENSP00000507303.1:n.-54+873C>T
ENST00000468682.2:n.436-1088C>T (HRAS)
ENST00000493230.5:c.-101C>T (HRAS)	ENSP00000434023.1:n.-101C>T
XM_011519875.1:c.-424-3135G>A (LRRC56)	XP_011518177.1:n.-424-3135G>A
XM_011519875.2:c.-424-3135G>A (LRRC56)	XP_011518177.1:n.-424-3135G>A
XM_011519877.1:c.-161-4117G>A (LRRC56)	XP_011518179.1:n.-161-4117G>A
XM_011519877.2:c.-161-4117G>A (LRRC56)	XP_011518179.1:n.-161-4117G>A
XM_017017167.1:c.-499-3060G>A (LRRC56)	XP_016872656.1:n.-499-3060G>A
XM_017017168.1:c.-499-3060G>A (LRRC56)	XP_016872657.1:n.-499-3060G>A
XR_242795.1:n.99C>T (HRAS)